Variant #0000518762 (NC_000003.11:g.191087711A>T, NM_178335.2:c.334A>T (CCDC50))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.191087711A>T
DNA change (hg38) g.191369922A>T
Published as CCDC50(NM_178335.2):c.334A>T (p.I112L)
ISCN -
DB-ID UTS2D_000002
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCDC50 NM_178335.2 ?/. - c.334A>T r.(?) p.(Ile112Leu)
UTS2D NM_198152.3 ?/. - c.-40173T>A r.(?) p.(=)


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